Methods for massive culture of dinophysis acuminata and isolation of pectenotoxin-2

ABSTRACT

Provided is a method for massive culture of  Dinophysis acuminata  which is a marine dinoflagellate causing diarrhetic shellfish poisoning, and methods for extracting, isolating and purifying the shellfish toxin pectenotoxin-2 from the cultured  Dinophysis acuminata.  Particularly,  Dinophysis acuminata  is cultured massively in massive culture apparatus comprising polycarbonate water bath having the bottom sinking down toward the center of the bottom; acryl tube (E) containing fluorescent lamp laid long in the center of the water bath; air supplying device (B) supplying the air to the sinking center of the bottom of the water bath; and air purifying device containing one or more devices selected from the group consisting of UV lamp (C) and carbon cartridge filter (D) purifying the air supplied by the said air supplying device.

CROSS-REFERENCE(S) TO RELATED APPLICATIONS

The present invention claims priority of Korean Patent Application No. 10-2008-0094357, filed on Sep. 25, 2008, which is incorporated herein by reference.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a method for massive culture of Dinophysis acuminata, the marine dinoflagellate causing diarrhetic shellfish poisoning, and methods for extracting, isolating and purifying the shellfish toxin pectenotoxin-2 from the cultured Dinophysis acuminata.

2. Description of Related Art

Dinophysis sp. belonging to dinoflagellates causing red tide is known to produce pectenotoxin (PTX) which is one of diarrhetic shellfish toxins. Once this organism causes red tide in the ocean, it brings huge damage on marine shellfish aquaculture. The major toxins produced by this living thing are okadaic acid, pectenotoxin, dinophysistoxin and yessotoxin, etc. It has been recently reported that pectenotoxin induces apoptosis selectively of cancer cells. So, expectation of medical or pharmaceutical usability of this material is increasing. In addition, pectenotoxin can be used as a standard material for toxin especially when red tide occurs by this living thing in the ocean. Although pectenotoxin has a wide spectrum of application, studies on the material have been limited for a long time because massive-culture of Dinophysis was unsuccessful and thus pectenotoxin could only picked up from a limited area.

Dinophysis acuminate, the marine dinoflagellate is a causing organism of diarrhetic shellfish poisoning which could not be cultured successfully in a lab until the year of 2006. The culture of Dinophysis acuminate was first succeeded by supplying laboratory culture of Myrionecta rubra, a marine ciliate, as feed in 2006 (Park et al. 2006. First successful culture of the marine dinoflagellate Dinophysis acuminate. Aquat. Microb. Ecol. 45, 101-106). Since then, success of culture of Dinophysis acuminate or other Dinophysis species using Myrionecta rubra has been reported from time to time.

However, the marine dinoflagellate, Dinophysis acuminate has been cultured only in a laboratory scale. So, the culture amount of Dinophysis acuminate is always not enough for the study of pectenotoxin, considering the increasing medical or pharmaceutical usability of the material. Therefore, a method for massive culture of Dinophysis acuminate is urgently requested for the study of pectenotoxin.

Based on the early method for culture of a small amount of Dinophysis acuminate, which was succeeded in a lab, the present inventors designed a simple water bath for massive culture of 500 liter and tried to establish a method for culture of the organism and a method for extracting and separating pectenotoxin, the diarrhetic shellfish toxin contained in the organism.

SUMMARY OF THE INVENTION

An embodiment of the present invention is directed to providing a method for massive culture of Dinophysis acuminate.

Another embodiment of the present invention is directed to providing a method for extracting and separating/purifying pectenotoxin-2 (PTX-2), the intracellular toxin of Dinophysis acuminate.

To achieve the objects of the present invention, the present invention provides a method for massive culture of Dinophysis acuminate, the marine dinoflagellate causing diarrhetic shellfish poisoning, and methods for extracting and separating/purifying pectenotoxin-2, the shellfish toxin included in Dinophysis acuminate.

Hereinafter, the present invention is described in detail.

The present invention relates to a method for massive culture of Dinophysis acuminate, the marine dinoflagellate causing diarrhetic shellfish poisoning, composed of the following 4 steps.

1) sub-culturing Myrionecta rubra at 10˜30° C. with continuous light, for which Myrionecta rubra and its prey Teleaulax are inoculated in sea water medium at the density ratio of 1:10-1:15;

2) inoculating Myrionecta rubra cultured in step 1) in the water bath supplied with the air purified by carbon cartridge filter after irradiation, and then mass-culturing Myrionecta rubra with stirring the cultured Myrionecta rubra in step 1) and the sea water medium using air bubbles formed and supplied through air sparging nozzle equipped on the lower part of the water bath at 10˜30° C. with continuous light;

3) inoculating Dinophysis acuminata and Myrionecta rubra, the prey for Dinophysis acuminata, at the density ratio of 1:10-1:30, followed by sub-culturing of Dinophysis acuminata at 10˜30° C. with continuous light;

4) mass-culturing Dinophysis acuminata by inoculating the Dinophysis acuminata cultured in step 3) in the water bath of step 2).

The sea water medium used for the massive culture of Dinophysis acuminata of the present invention includes any conventional medium used for the culture of algae except diatoms, for example f/2-Si medium, particularly 30 psu (practical salinity unit) f/2-Si medium.

The massive culture apparatus for massive culture of Dinophysis acuminata comprising 500 liter water bath and its parts are illustrated in FIG. 1. This apparatus for massive culture of Dinophysis acuminata can also be used for massive culture of other kinds of plant planktons.

Massive culture of Dinophysis acuminata of the present invention, particularly massive culture in step 2) or step 4) is performed in massive culture apparatus comprising polycarbonate water bath having the bottom sinking down toward the center of the bottom; acryl tube (E) containing fluorescent lamp laid long in the center of the water bath; air supplying device (B) supplying the air to the sinking center of the bottom of the water bath; and air purifying device containing one or more devices selected from the group consisting of UV lamp (C) and carbon cartridge filter (D) purifying the air supplied by the said air supplying device (FIG. 1).

The water bath of the massive culture apparatus has the volume of at least 500 liter and is made round of more than 0.8 m diameter from polycarbonate plate emitting least toxic materials, whose bottom is sinking to the center of the bottom part. This water bath, therefore, suits for harvest of Dinophysis acuminata massively cultured and is easy to clean and drain. The top of the bath is covered by a lid to prevent foreign materials from coming in. The height of the bath is at least 1 m. The ratio of cylindrical part to conical part is 2:1-3:2. The diameter of this bath is at least 0.8 m, which favors receiving light enough.

This apparatus also contains culture medium for massive culture, precisely sea water medium, and acryl tube with a built-in fluorescent lamp (32 watt, 120 cm long) laid long in the center of the bath to supply light to the target organism evenly, which makes the plant do photosynthesis effectively. It also includes air supplying device (B) composed of air supplying part supplying air to the sinking center part of the bottom of water bath, connection tube and sparging nozzle, and air purifying device containing one or more devices selected from the group consisting of UV lamp and carbon cartridge filter (D) purifying the air supplied by the said air supplying device.

Small bubbles are formed from the sinking center part of the bottom of the water bath by the sparging nozzle in the air supplying device.

Dinophysis acuminata massively cultured by the said method can be recovered by ultra centrifuge (F) connected to the sinking center part of the bottom of the water bath.

The result of massive culture of Dinophysis acuminata using the massive culture apparatus of the present invention is illustrated in FIG. 2.

In the method of the present invention, to culture Dinophysis acuminata and its prey Myrionecta rubra massively, 100 M

of seed strain was first cultured to 2

, followed by sub-culture as follows; 2

to 20

and 20

to 500

. At this time, inoculation ratio of Myrionecta rubra to its prey Teleaulax was 1:10-1:15 and inoculation ratio of Dinophysis acuminata to its prey Myrionecta rubra was 1:10-1:30. To increase maximum density of Dinophysis acuminata, ⅕ of sea water medium was discarded when the prey Myrionecta rubra was consumed and then fresh sea water medium was preferably added together with Myrionecta rubra the prey thereto.

Further, the present invention provides methods for harvesting Dinophysis acuminata massively cultured from the sea water medium using ultra centrifuge (F) connected to the fallen center part of the bottom of the water of the massive culture apparatus, for separating and purifying the toxin, pectenotoxin-2 (FIG. 3), from the harvested Dinophysis acuminata using solvent distribution and chromatography. The separated and purified pectenotoxin-2 was confirmed by mass spectrometer and NMR. The mass analysis data obtained therefrom (FIG. 4) and hydrogen and carbon spectrums (FIG. 5 and FIG. 6) are shown in the attached Fig.s and chemical shifts of hydrogen and carbon of pectenotoxin-2 are shown in FIG. 7.

The solvent distribution herein is performed by the following steps: extracting with solvent using butanol solution; concentrating the alcohol extract, followed by solvent fractionation using methanol/water/-n-hexane mixture composed of the volume ratio of 1:5˜6:6˜7; and concentrating the solvent fractionated layer composed of methanol and water. Upon completion of the solvent distribution, chromatography is performed. Precisely reverse-phased silica flash chromatography and reverse-phased semi-preparative HPLC are performed stepwise to separate/purify pectenotoxin-2.

Reverse-phased silica flash chromatography uses reverse phase silica gel as immobile phase and uses water/methanol (1:1˜9, V/V) mixture, methanol and acetone as eluents. More preferably, the mixture of water and methanol (1:4, V/V) is used as eluent. Effluent from reverse-phased silica flash chromatography is concentrated, followed by reverse-phased semi-preparative HPLC using column filled with reverse-phased silica gel (C18) and eluent which is the mixture of methanol (75%) and water (25%). Pectenotoxin-2 is extracted at retention time of 59 minutes.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 illustrates the 500

massive culture apparatus for Dinophysis acuminata culture. A: power supply, B: air supplying device to supply air, C: UV lamp to sterilize the supplied air, D: carbon cartridge filter to filter the supplied air, E: 32 watt fluorescent lamp, and F: ultra centrifuge to harvest the cultured organism.

FIG. 2 is a graph illustrating the changes of cell densities of Dinophysis acuminata and the prey Myrionecta rubra observed for 8 days of massive culture (500

) of Dinophysis acuminata in Example 1.

FIG. 3 illustrates the chemical structure of the pectenotoxin-2 separated and purified from Dinophysis acuminata.

FIG. 4 illustrates the mass spectrometry data of the pectenotoxin-2 separated and purified in Example 2.

FIG. 5 illustrates the hydrogen NMR spectrometry data of the pectenotoxin-2 separated and purified in Example 2.

FIG. 6 illustrates the carbon NMR spectrometry data of the pectenotoxin-2 separated and purified in Example 2.

FIG. 7 is a table showing the hydrogen and carbon NMR lines designated in the molecular structure of the pectenotoxin-2 separated and purified in Example 2.

DESCRIPTION OF SPECIFIC EMBODIMENTS

The advantages, features and aspects of the invention will become apparent from the following description of the embodiments with reference to the accompanying drawings, which is set forth hereinafter.

Example 1 Massive Culture of Dinophysis Acuminate

To culture Dinophysis acuminate, the ciliate Myrionecta rubra the prey for Dinophysis acuminate, and the cryptomonad Teleaulax, the prey for Myrionecta rubra, had to be first cultured enough. For the culture of these two preys, the present inventors referred the literature (Yih et al. 2004. Ingestion of cryptophyte cells by the marine photosynthetic ciliate Mesodinium rubrum. Aquat. Microb. Ecol. 36:165-170) informing the size of experiment (small scale, 500 M

) and then cultured 100 M

sized laboratory seed strain up to 2

which was then sub-cultured to 20

. The cultured seed strain was inoculated in massive culture apparatus containing 500

water bath and grown for 1 week until Dinophysis acuminate was inoculated. At that time, the ratio of the seed strain to its prey Teleaulax was 1:10-1:15. The culture was performed in f/2-Si medium at 20° C. with salt concentration of 30 psu and with continuous light at the luminosity of 60 photon/m²/sec. The seed strain was sub-cultured when the maximum cell density reached 10,000 cells/M

.

For massive culture of Dinophysis acuminata with 500

scale, small scale (100 M

) of laboratory seed strain was first cultured with increasing the volume from 2

to 20

gradually. The ratio of Dinophysis acuminata to its prey Myrionecta rubra was adjusted to 1:30 at the initial inoculation. Sub-culture interval was 5-10 days. When the maximum density of Dinophysis acuminata reached 2,000 cells/M

, it was inoculated into a larger culture vessel. The culture was performed in f/2-Si medium at 20° C. with salt concentration of 30 psu and with continuous light at the luminosity of 60 photon/m²/sec. When Dinophysis acuminata grew to 20

, it was inoculated into the massive culture apparatus containing 500

water bath wherein the prey Myrionecta rubra had been growing for a week. On day 6, when the prey Myrionecta rubra was all consumed and the density of Dinophysis acuminata reached about 3,000 cells/M

, ⅕ of sea water medium was discarded and Myrionecta rubra which was growing in a separate 20

culture vessel was supplied and fresh sea water medium was also added. Then, when the maximum density of Dinophysis acuminata reached about 5,000 cells/M

, harvest was performed (FIG. 2).

Example 2 Separation and Purification of Pectenotoxin-2 from Dinophysis acuminata

After culturing Dinophysis acuminata to 500

in a lab, 100 g (wet weight) of the biomass was harvested using continuous centrifuge (flow rate: 3

/min, 6000 rpm). The obtained organism was freeze-dried for 3 days, then 3.0

of methanol was added thereto, which stood for 48 hours, followed by extracting organic material. The solvent was removed from the extract using rotary evaporator, to which the mixed solution composed of butanol and water (1:1) was added, followed by solvent distribution to separate water layer and butanol layer. Butanol was eliminated from the butanol layer obtained by the solvent distribution using vacuum evaporator, to which the mixture composed of methanol (15%) and water (85%) and n-hexane (1:1) were added, followed by redistribution. Next, the solvent layer composed of methanol and water was separated, and then the solvent was eliminated by the same method described above. The obtained fraction proceeded to reverse-phased silica flash chromatography. At this time, reverse-phased silica gel (C-18) was used as immobile phase. The eluent was used in the order of high polarity to lower polarity. Particularly, the order was as follows and the amount of organic material obtained was as described: 50% water/50% methanol (300 mg), 40% water/60% methanol (200 mg), 30% water/70% methanol (10 mg), 20% water/80% methanol (10 mg), 10% water/90% methanol (50 mg), 100% methanol (240 mg), 100% acetone (230 mg). Spectrum was measured with each fraction obtained by the above method using hydrogen NMR spectrometer. As a result, it was confirmed that approximately 70% of pectenotoxin-2 was included in the layer of 20% water/80% methanol. So, organic solvent was eliminated from the fraction containing pectenotoxin-2 using vacuum evaporator, followed by reverse-phased semi-prep HPLC to purify the major component pectenotoxin-2. Conditions for HPLC were as follows. column: YMC ODS-C18, particle diameter: 5 μm, column size: 250 10 mm (length diameter), elution rate: 1.5 M

/min, detector: refractive index detector, and eluent: 75% methanol/25% H₂O. As a result, grey powder pectenotoxin-2 was separated at retention time of 59 minutes.

To confirm the pectenotoxin-2 finally obtained, liquid chromatography-mass spectrometer (LC-MS) and nuclear magnetic resonance (NMR) spectrometer were used. From the liquid chromatography-mass spectrometry was confirmed the molecular weight signals indicating pectenotoxin having the molecular weight of 858 and the one containing H₂O and thus having the molecular weight of 876 (M+H₂O). 1D and 2D NMR spectrometry was performed with pectenotoxin-2 to identify the chemical structure, which was as described previously. Liquid chromatography-mass spectrometry data (FIG. 4) and hydrogen and carbon NMR spectrums (FIG. 5 and FIG. 6) were presented. FIG. 7 illustrates signals shown on hydrogen and carbon NMR spectrums of pectenotoxin-2.

Owing to the method for massive culture of Dinophysis acuminata of the present invention, the inventors succeeded the culture of acuminata, one of Dinophysis species, up to 500 liter, which had been unsuccessful until then. Pectenotoxin separated from Dinophysis acuminata can be not only used as a standard toxin for the analysis of toxins but also used for the study to fight cancer which is actively going on more than ever, suggesting that this material is a promising candidate for the medically pharmaceutically usable material.

While the present invention has been described with respect to the specific embodiments, it will be apparent to those skilled in the art that various changes and modifications may be made without departing from the spirit and scope of the invention as defined in the following claims. 

1. A method for massive culture of Dinophysis acuminate, comprising; sub-culturing Myrionecta rubra at 10˜30° C. with continuous light, for which Myrionecta rubra and its prey Teleaulax are inoculated in sea water medium at the density ratio of 1:10-1:15; inoculating Myrionecta rubra cultured in the sub-culturing of Myrionecta rubra in the water bath supplied with the air purified by carbon cartridge filter after irradiation, and then mass-culturing Myrionecta rubra with stirring the cultured Myrionecta rubra in the sub-culturing of Myrionecta rubra and the sea water medium using air bubbles formed and supplied through air sparging nozzle equipped on the bottom part of the water bath at 10˜30° C. with continuous light; inoculating Dinophysis acuminate and Myrionecta rubra, the prey for Dinophysis acuminate, at the density ratio of 1:10-1:30, followed by sub-culturing of Dinophysis acuminate at 10˜30° C. with continuous light; and mass-culturing Dinophysis acuminate by inoculating the Dinophysis acuminate cultured in the sub-culturing of Dinophysis acuminate in the water bath of the mass-culturing of Myrionecta rubra.
 2. The method for massive culture of Dinophysis acuminate according to claim 1, wherein the sea water medium is f/2-Si.
 3. The method for massive culture of Dinophysis acuminata according to claim 1, wherein the massive culture in the mass-culturing of Myrionecta rubra or the mass-culturing of Dinophysis acuminata is performed in massive culture apparatus comprising polycarbonate water bath having the bottom sinking down toward the center of the bottom; acryl tube (E) containing fluorescent lamp laid long in the center of the water bath; air supplying device (B) supplying the air to the sinking center of the bottom of the water bath; and air purifying device containing one or more devices selected from the group consisting of UV lamp (C) and carbon cartridge filter (D) purifying the air supplied by the said air supplying device.
 4. A method for separating pectenotoxin-2 from Dinophysis acuminata using solvent distribution and chromatography.
 5. The method for separating pectenotoxin-2 according to claim 4, wherein the solvent distribution is performed as follows; extracting with solvent using butanol aqueous solution; concentrating the alcohol extract, followed by solvent fractionation using methanol/water/normal hexane mixture composed of the ratio of 1:5˜6:6˜7; and concentrating the solvent fractionated layer composed of methanol and water.
 6. The method for separating pectenotoxin-2 according to claim 4, wherein the chromatography is performed by reverse-phased silica flash chromatography and reverse-phased semi-preparative HPLC after solvent distribution.
 7. The method for separating pectenotoxin-2 according to claim 6, wherein the reverse-phased silica flash chromatography uses reverse-phased silica gel as immobile phase and uses water/methanol (1:1˜9, V/V) mixture, methanol and acetone as eluents.
 8. The method for separating pectenotoxin-2 according to claim 7, wherein the eluent for the reverse-phased silica flash chromatography is the mixed solution of water and methanol (1:4, V/V).
 9. The method for separating pectenotoxin-2 according to claim 6, wherein the reverse-phased semi-preparative HPLC is performed using column filled with reverse-phased silica gel (C18) and eluent composed of methanol (75%) and water (25%).
 10. The method for separating pectenotoxin-2 according to claim 9, wherein the pectenotoxin-2 is extracted at retention time of 59 minutes. 